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Niaspan
Niaspan - 21695-865-90 - (Niacin)
Drug Information of Niaspan
| Product NDC: | 21695-865 |
| Proprietary Name: | Niaspan |
| Non Proprietary Name: | Niacin |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Niacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Niaspan
| Product NDC: | 21695-865 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020381 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970728 |
Package Information of Niaspan
| Package NDC: | 21695-865-90 |
| Package Description: | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-865-90) |
NDC Information of Niaspan
| NDC Code | 21695-865-90 |
| Proprietary Name | Niaspan |
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-865-90) |
| Product NDC | 21695-865 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Niacin |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19970728 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | NIACIN |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient] |
